Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.
- NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_assertion description "[We conclude that PEX7 is responsible for RCDP (PBD CG11) and suggest a founder effect may explain the high frequency of L292ter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.
- NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_assertion evidence source_evidence_literature NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.
- NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_assertion SIO_000772 9090381 NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.
- NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_assertion wasDerivedFrom befree-20140225 NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.
- NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_assertion wasGeneratedBy ECO_0000203 NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP186398.RAwqY_BeKbyMSa7mSraU46ER-vCxX3X98WArFr9p78hdc130_provenance.